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1  spectrotemporal modulations in the songs of zebra finches).
2 nse elements in orthologous promoters in the zebra finch.
3 ion in the developing embryonic beaks of the zebra finch.
4 s been retained in other bird lineages, like zebra finch.
5 ound in another avian lineage, the passerine zebra finch.
6 umber of brain regions were activated in the zebra finch.
7 erally available cell lines derived from the zebra finch.
8 a high-resolution genetic linkage map of the zebra finch.
9 mparative maps of the genomes of chicken and zebra finch.
10 phalic enlargement in passerines such as the zebra finch.
11 lls in a vocal learning Neoaves species, the zebra finch.
12  sparrow and was essentially undetectable in zebra finch.
13  similar, suggesting no heterochiasmy in the zebra finch.
14 the NCL in pigeon, chicken, carrion crow and zebra finch.
15 y/associative forebrain of the highly social zebra finch.
16 of the avian vocal organ, the syrinx, in the zebra finch.
17  that ketolation occurs in the integument in zebra finches.
18 oxP2 disrupts song learning in juvenile male zebra finches.
19 ise known for being essential for singing in zebra finches.
20 erization that could impact song behavior in zebra finches.
21 identified HVC projection neurons in singing zebra finches.
22 protein in brains of juvenile and adult male zebra finches.
23  controls learning and production of song in zebra finches.
24 thalamofugal and the tectofugal pathways, of zebra finches.
25  dynamic control of subsyringeal pressure in zebra finches.
26 log FoxP2 disrupts song learning in juvenile zebra finches.
27  upper-vocal-tract filtering to the songs of zebra finches.
28 generated neurons into the brain of juvenile zebra finches.
29 ingle HVC axons innervating RA in adult male zebra finches.
30 essary for vocal variability and learning in zebra finches.
31 nctionally changes over vocal development in zebra finches.
32 ing, we analyzed the songs of young juvenile zebra finches.
33 f complex, learned acoustic signals in awake zebra finches.
34 an elegant ability for red discrimination in zebra finches.
35 of the arcopallium in brain slices from male zebra finches.
36 rial sections in embryonic and post-hatching zebra finches.
37 ed lentivirus to produce germline transgenic zebra finches.
38 ed in NIf and HVC of anesthetized adult male zebra finches.
39  whether a comparable transmission occurs in zebra finches.
40 n vocal production learning in juvenile male zebra finches.
41 computational complexity of song learning in zebra finches.
42 physiological studies of selected neurons in zebra finches.
43 n the auditory and sensorimotor forebrain of zebra finches.
44 eural processing of vocal sounds, using male zebra finches.
45 r characterization of the arcopallium in the zebra finch, a passerine songbird species and a major mo
46 and chronic recording methods in the singing zebra finch, a small songbird that relies on auditory fe
47 tnap2 protein expression in the brain of the zebra finch, a songbird species in which males, but not
48                                          The zebra finch, a songbird, presents a unique opportunity t
49  programs in the four key song nuclei of the zebra finch, a vocal learning songbird.
50                     Here, in male and female zebra finches, a combination of aromatase immunohistoche
51 ive during call-based vocal communication of zebra finches, a highly social songbird species.
52 he present study we actively immunized adult zebra finches against VIP conjugated to KLH and compared
53                      Furthermore, within the zebra finch, all receptors, except for D4, showed differ
54                                          The zebra finch also does not show the reduced male-to-femal
55  characterize transcript distribution in the zebra finch, an experimentally tractable songbird for wh
56 ate important differences in the PGCs of the zebra finch and advance the first stage of creating PGC-
57 all structures of the genomes are similar in zebra finch and chicken, but they differ in many intrach
58                                      In both zebra finch and chicken, the D1A, D1B, and D2 receptors
59 ies being found in chicken, turkey, duck and zebra finch and its expression profile confirmed in both
60 pulation in Africa, and tens of genomes from zebra finch and long-tailed finch populations in Austral
61                                              Zebra finch and rat CBG crystal structures in complex wi
62                       One is inspired by the zebra finch and successfully reproduces songbird singing
63 of 8,424 orthologs in both falcons, chicken, zebra finch and turkey identified consistent evidence fo
64 at a social feedback loop between young male zebra finches and adult females guides the process of so
65                                   Studies in zebra finches and canaries have now identified the gene
66 ture functional studies we cloned FoxP4 from zebra finches and compared regional and cellular coexpre
67 gulated FoxP1 or FoxP4 in Area X of juvenile zebra finches and compared the resulting song phenotypes
68                                           In zebra finches and other songbirds, there is a sensitive
69 hicle was administered peripherally to adult zebra finches and sickness behavior was recorded 2 or 24
70 ous measurement of neuronal activity of male zebra finches and vocalizations of males and females tha
71 udy we tested these abilities in a songbird (zebra finch) and a parrot species (budgerigar).
72 ional and experimental data from chicken and zebra finch, and acts to equalize male-to-female express
73 ve immune gene repertoire, as in chicken and zebra finch, and this repertoire has been shaped through
74 m neurons in area X of singing juvenile male zebra finches, and directly compared their firing patter
75 energic receptors was investigated in quail, zebra finches, and rats.
76 postnatal auditory environment of developing zebra finches, and then assessed effects on hemispheric
77 llular basis of telencephalic enlargement in zebra finches, and then to compare these findings with w
78 ert multiple long-term phenotypic effects in zebra finches, and we here test for effects of these man
79  nucleus LMAN during development as juvenile zebra finches are actively engaged in evaluating feedbac
80 te experimentally that the songs of juvenile zebra finches are guided toward mature vocal forms by re
81                                              Zebra finches are widely used for studying the basic bio
82 at single neurons, in the auditory cortex of zebra finches, are capable of discriminating the individ
83 nglia-projecting dopamine neurons in singing zebra finches as we controlled perceived song quality wi
84  from this work is that the telencephalon of zebra finches at hatching contains a thick proliferative
85     Here, we infused norepinephrine into the zebra finch auditory cortex and performed extracellular
86 , we describe a population of neurons in the zebra finch auditory cortex that represent vocalizations
87 pectrograms by combining the spike trains of zebra finch auditory midbrain neurons with information a
88 osome painting and cytogenetic mapping of 15 zebra finch BAC clones to the standard (ZAL2) and altern
89 is enrichment in song control neurons of the zebra finch basal ganglia impairs tutor song imitation,
90                  We end-sequenced cDNAs from zebra finch brain and incorporated additional sequences
91                          Here we cloned from zebra finch brain cDNAs of all avian dopamine receptors:
92                                          The zebra finch brain features a set of clearly defined and
93                            This atlas of the zebra finch brain is expected to become an important too
94 VZ cell proliferation, male and female adult zebra finch brain slices containing the VZ were exposed
95                         Recording from adult zebra finch brain slices we show that within each bird b
96                Cntnap2 protein expression in zebra finch brain supports the hypothesis that this mole
97 iour engages gene regulatory networks in the zebra finch brain, altering the expression of long non-c
98 erved in a high-level auditory region of the zebra finch brain, we addressed this question at the neu
99 tein expression in song-related areas of the zebra finch brain.
100 secondary auditory cortex-like region of the zebra finch brain.
101 d an acute regulation of auditory neurons in zebra finches by (1) delineating the extent of the brain
102 ulated NR2B expression in LMAN of adult male zebra finches by increasing its protein levels to those
103 cts on RA projection neurons, but that adult zebra finches can partially compensate for this deficit
104 nd that the dopaminergic reward circuitry of zebra finches can simultaneously promote social cohesion
105                                              Zebra finches categorized test stimuli with previously h
106 term potentiation, is rapidly induced within zebra finch caudal medial nidopallium (NCM) following no
107 main site of plasma CBG production, and anti-zebra finch CBG antibodies cross-react with CBGs in othe
108          Glycosylation of this asparagine in zebra finch CBG does not influence its steroid-binding a
109                                  Recombinant zebra finch CBG steroid-binding properties reflect those
110          Substitutions of amino acids within zebra finch CBG that are conserved only in birds reveal
111 the dynamics of Hoxb genes activation during zebra finch, chicken, and ostrich gastrulation, we provi
112                            Here we show that Zebra Finch chicks (Taeniopygia guttata) are capable of
113                                              Zebra finches communicate with each other in ways that a
114                    Like other songbirds, the zebra finch communicates through learned vocalizations,
115 neural tracers in the TeO and the Ipc of the zebra finch demonstrated that neurons from the external
116 neuroestrogen levels in the forebrain of the zebra finch depend on calcium influx within presynaptic
117                    This study shows that the zebra finch differs from the chicken because it lacks a
118 he oculomotor cerebellum in hummingbirds and zebra finches do not originate in the medial LM (as in p
119          We found that subsong production in zebra finches does not require HVC (high vocal center),
120 uit is enhanced in male compared with female zebra finches due to differential rates of incorporation
121  Imaging with song analyses in juvenile male zebra finches during song learning and beyond, we reveal
122 rds (chicken, duck, pigeon, ostrich, emu and zebra finch), early postnatal marsupial mammals (fat-tai
123     Additional experiments in the gregarious zebra finch (Estrildidae: Taeniopygia guttata) underscor
124                     In the highly gregarious zebra finch (Estrildidae: Taeniopygia guttata), blockade
125                     We now show that in male zebra finches (Estrildidae: Taeniopygia guttata), Fos ac
126 ffect of ovulation order on TL in embryos of zebra finches experiencing the same controlled incubatio
127                                      In male zebra finches, experimental manipulation of FoxP2 in Are
128 ripheral tissues (liver, spleen, and fat) of zebra finches exposed to 12 h light:12 h darkness (LD),
129 vaeformis (Uva) of the posterior thalamus in zebra finches extend farther rostrally than to Uva, as g
130 vaeformis (Uva) of the posterior thalamus in zebra finches extend farther rostrally than to Uva, as g
131 w well neural spike trains recorded from the zebra finch field L (an analog of mammalian primary audi
132 s tested song responsiveness of adult female zebra finches for three acoustically different song type
133                                          The zebra finch, for example, sings a highly stereotyped son
134 und that activation of HTR2 receptors in the zebra finch forebrain song premotor structure the robust
135  sequences in HVC (proper name) of the adult zebra finch forebrain that are central to the performanc
136 ivo intracellular recordings in anesthetized zebra finches from the input (nucleus HVC, used here as
137             A complete draft sequence of the zebra finch genome is imminent, yet a need remains for a
138 ing path microarray and identify CNVs in the zebra finch genome relative to chicken; 32 interspecific
139                                Access to the zebra finch genome sequence will, therefore, prompt new
140                                The wild-type zebra finch genome was found to have three intact genes
141 apped the majority to the recently assembled zebra finch genome.
142 aping patterns of molecular evolution in the zebra finch genome.
143 arrangements were reported; (2) to hybridize zebra finch genomic DNA to a chicken tiling path microar
144                             We show that the zebra finch GRC contains >115 genes paralogous to single
145 st exploited differences between chicken and zebra finch gut morphology to identify the BMP pathway a
146                 Although transgenesis in the zebra finch has been accomplished, it is with a very low
147                                          The zebra finch has been used as a valuable vocal learning a
148                                          The zebra finch has long been an important model system for
149  to its basal ganglia part, Area X, in adult zebra finches has been noted to have no strong effects o
150                           Songbirds like the zebra finch have become important models to understand t
151 eginning of the sensitive period, just after zebra finches have fledged from the nest, there is an in
152 nderstand this phenomenon better, we studied zebra finches hearing playbacks of birdsong.
153         This circuit is incomplete in female zebra finches, hence only males sing.
154    The addition of HVC-RA neurons happens in zebra finches housed singly, but becomes more acute if t
155  in seasonal songbirds, neurons added to the zebra finch HVC are not part of a replacement process.
156 onses to intracellular current injections of zebra finch HVC neurons.
157      Here we examined the circuit anatomy of zebra finch HVC, a cortical region that generates sequen
158 emotor cortex (HVC, acronym is name) in male zebra finches identified prominent efferent pathways fro
159 tire chromosomes between chicken, turkey and zebra finch, identifying syntenic blocks of at least 250
160                                          The zebra finch is an important model organism in several fi
161 h the imminent sequencing of its genome, the zebra finch is now poised to become a model system for p
162                    The neural song system in zebra finches is highly sexually dimorphic; only males s
163                                              Zebra finch isolates, unexposed to singing males during
164                       We found that juvenile zebra finches living in flocks socially learned novel fo
165 supports 51 species including marmoset, pig, zebra finch, lizard, gorilla and wallaby, which were add
166                            We found that the zebra finch LSt projects to the GP, substantia nigra par
167 te early gene ZENK) during sleep in juvenile zebra finch males that were still learning their songs f
168 , a letter-based name) of juvenile and adult zebra finch males, independent of the song stimulus pres
169                     Here we show that in the zebra finch, many auditory midbrain neurons have extra-c
170                   The elastic modulus of the zebra finch ML is 18 kPa at 5% strain, which is comparab
171       Here, we addressed these issues in the zebra finch model by combining intracerebral pharmacolog
172 halamus exerts diverse behavioral effects in zebra finches, most of which are sexually differentiated
173               We measured telomere length in zebra finches (n = 99) from the nestling stage and at va
174  Much as children learn language, young male zebra finches need to interact socially with an adult tu
175                                 In the adult zebra finch, new projection neurons are added to the nuc
176                     Birdsong learning in the zebra finch occurs during a sensitive period similar to
177 aHVC based on expression of zRalDH for adult zebra finches of both sexes and for males during the son
178 n-specific neuronal activation in the VMH of zebra finch parents.
179        Here, we show, however, that juvenile zebra finches partway through song learning, singing imm
180 roved conditions for isolating and culturing zebra finch PGCs in vitro and were able to transfect the
181 rences between the 2 species, including that zebra finch PGCs were more numerous, more widely distrib
182 ted by Pseudomonas aeruginosa cleaves CBG in zebra finch plasma within its reactive center loop and d
183  field L (primary auditory cortex analog) of zebra finches, previous studies identified a limited set
184                                        Thus, zebra finches prioritize efficient learning of syllable
185 es for two bird species, the chicken and the zebra finch, provides, for the first time, an ideal oppo
186 mutual mate choice in captive populations of Zebra finches (r = -0.020, 95% CI -0.148-0.107, 1,414 pa
187 lencephalic neurogenesis are both delayed in zebra finches relative to quail (Galliformes).
188         Dopaminergic neurons in anesthetized zebra finches respond more strongly to the bird's own so
189                                   A study of zebra finches reveals the potential advantages of idiosy
190 output nucleus of this circuit in adult male zebra finches reverses moderate changes in song structur
191                                       In the zebra finch, singing behavior is driven by a sequence of
192 g techniques, on their ability to identify a zebra finch song in the presence of a background masker
193 thin the spectral and temporal dimensions of zebra finch song structure.
194 und in a long sequence of sounds (canary and zebra finch song syllables) patterned in either an alter
195 sms regulating sexual differentiation of the zebra finch song system appear to include both genetic a
196 e-related morphological changes in the adult zebra finch song system by focusing on two cortical proj
197 esponsible for sexual differentiation of the zebra finch song system remains unknown but likely invol
198 modulate the sexually differentiation of the zebra finch song system.
199 recisely timed learned motor sequence, adult zebra finch song, to examine motor preparation.
200 ent amounts of statistical information about zebra finch song.
201 s have been reported in adult and developing zebra finch song.
202 in ovo in poultry, and apply it to posthatch zebra finch songbird chicks.
203                                Juvenile male zebra finch songbirds (females cannot sing) learn to sin
204       Here, we investigated mTOR in juvenile zebra finch songbirds.
205 tions matched to those found across multiple zebra finch songs to yield song spectrograms similar to
206 thms of wild thrush nightingale and domestic zebra finch songs.
207                               Recent work in zebra finches suggests that genes and hormones may act t
208 , mounting evidence in one such species, the zebra finch, suggests that forms of plasticity common du
209 opy to optically section oviduct tissue from zebra finch Taeniopygia guttata females label free by ha
210 ow that inbreeding causes early death in the zebra finch Taeniopygia guttata, and among inbred indivi
211                            A comparison with zebra finch Taeniopygia guttata, chicken Gallus gallus a
212  in the caudomedial nidopallium (NCM) of the zebra finch (Taeniopygia guttata) brain.
213 ined myelin development in the brains of the zebra finch (Taeniopygia guttata) from chick at posthatc
214                 The recent sequencing of the zebra finch (Taeniopygia guttata) genome allowed an asse
215 kers against the chicken (Gallus gallus) and zebra finch (Taeniopygia guttata) genomes places the Ppu
216                                 A young male zebra finch (Taeniopygia guttata) learns to sing by copy
217   Here we use the yellowbeak mutation in the zebra finch (Taeniopygia guttata) to investigate the gen
218 describe a genome-wide analysis of LD in the zebra finch (Taeniopygia guttata) using 838 single nucle
219 alysis of a whole-genome linkage map for the zebra finch (Taeniopygia guttata) using a 354-bird pedig
220 lation of Cck in the brain of the adult male zebra finch (Taeniopygia guttata), a songbird species.
221 the first evidence that song learning in the zebra finch (Taeniopygia guttata), the most common model
222 hroated sparrow (Zonotrichia albicollis) and zebra finch (Taeniopygia guttata), we labeled putative V
223 ative analysis of the genome sequence of the zebra finch (Taeniopygia guttata), which is a songbird b
224 y, we investigated a passerine songbird, the zebra finch (Taeniopygia guttata), with a biparental car
225 bird species: the pigeon (Columba livia) and zebra finch (Taeniopygia guttata).
226 e extend such an analysis to a songbird, the zebra finch (Taeniopygia guttata).
227 histological sections from the brain of male zebra finches (Taeniopygia guttata) and make them public
228                                         Male zebra finches (Taeniopygia guttata) are vocal learners t
229 udomedial auditory forebrain of anesthetized zebra finches (Taeniopygia guttata) at 32 sites simultan
230  we recorded the vocalisations of individual zebra finches (Taeniopygia guttata) behaving freely in s
231 emotor nucleus HVC (proper name) in juvenile zebra finches (Taeniopygia guttata) during auditory lear
232 tory inputs from vocal effectors of juvenile zebra finches (Taeniopygia guttata) during the stage of
233 ow that short bouts of singing in adult male zebra finches (Taeniopygia guttata) induce persistent in
234                 Song development in juvenile zebra finches (Taeniopygia guttata) is characterized by
235 ors found that song responsiveness in female zebra finches (Taeniopygia guttata) is strongly modulate
236                                              Zebra finches (Taeniopygia guttata) learn to produce son
237                             Song learning in zebra finches (Taeniopygia guttata) requires exposure to
238    New neurons are added, too, to the HVC of zebra finches (Taeniopygia guttata) that do not learn ne
239  a model for a migrating songbird, we fasted zebra finches (Taeniopygia guttata) that had been dosed
240               In the vocal control system of zebra finches (Taeniopygia guttata) the pre-motor mechan
241 photon calcium imaging in anesthetized adult zebra finches (Taeniopygia guttata) to examine how learn
242 rners, combining an experimental approach in zebra finches (Taeniopygia guttata) with an analysis of
243 d-eared turtles (Trachemys scripta elegans), zebra finches (Taeniopygia guttata), and mice (Mus muscu
244  between Anna's hummingbirds (Calypte anna), zebra finches (Taeniopygia guttata), and pigeons (Columb
245                           We PIT-tagged wild zebra finches (Taeniopygia guttata), monitoring their re
246                      The songs of adult male zebra finches (Taeniopygia guttata), produced as rapid s
247                                     In adult zebra finches (Taeniopygia guttata), the telencephalon o
248                                 Adult female zebra finches (Taeniopygia guttata), which do not produc
249 e temporal structure of learned song in male zebra finches (Taeniopygia guttata).
250 ellular recordings of HVC neurons in singing zebra finches (Taeniopygia guttata).
251 enriched in the song control system of adult zebra finches (Taeniopygia guttata).
252 involved with the regulation of immunity, in zebra finches (Taeniopygia guttata).
253 ame) encodes the learned songs of adult male zebra finches (Taeniopygia guttata).
254  resequencing data for two bird species: the zebra finch, Taeniopygia guttata, and the long-tailed fi
255 ion of CART-immunoreactivity in the brain of zebra finch, Taeniopygia guttata, its interaction with N
256 basal ganglia circuit of juvenile songbirds (zebra finches, Taeniopygia guttata) during vocal learnin
257  in prairie voles (Microtus ochrogaster) and zebra finches (Taenioypygia guttata), and also reduces t
258 onlinear dynamics to test whether adult male zebra finches (Taenopygia guttata) use the intrinsic non
259  We developed germline transgenic songbirds, zebra finches (Taneiopygia guttata) expressing human mut
260                   These results suggest that zebra finches' tectofugal pathway predominately processi
261 n mRNA was widely distributed throughout the zebra finch telencephalon, overlapping with song control
262 nd learning-related (Area X) song regions of zebra finch telencephalon.
263 sumptive tectum is proportionally smaller in zebra finches than quail before neurogenesis begins, thi
264         In this study, we show that in young zebra finches that are just beginning to learn the struc
265 g stereotypy is persistently reduced in male zebra finches that have been developmentally exposed to
266  avian cortical auditory neurons recorded in zebra finches that were listening to a large set of call
267 ere we investigated in a songbird model, the zebra finch, the neural substrate for ranging and identi
268                  Measurements of CBG mRNA in zebra finch tissues indicate that liver is the main site
269                                   We exposed zebra finches to aversively reinforcing white noise stim
270 ork analysis on microarray data from singing zebra finches to discover gene ensembles regulated durin
271              We manipulated song learning in zebra finches to experimentally control the requirements
272 oped a spatial orientation assay and trained zebra finches to magnetic and/or overhead polarized ligh
273                              We exposed male zebra finches to tutor or unfamiliar song.
274 phogen Sonic hedgehog (SHH) in the chick and zebra finch, two species that differ in size during the
275 the ascending projections of the nTTD in the zebra finch, using in vivo injections of biotinylated de
276 a size) within brain regions associated with zebra finch vocal learning are affected by late-postnata
277  situ hybridization effort, we show that the zebra finch vocal robust nucleus of the arcopallium (RA)
278  the lateral septum, and sociality in female zebra finches was reduced by OT antagonist infusions int
279     To improve germ-line transmission in the zebra finch, we identified and characterized its primord
280                     In both carrion crow and zebra finch, we identified four different subareas of hi
281    Using intracellular recordings in singing zebra finches, we found that DAF failed to perturb singi
282                                           In zebra finches, we found that exposure to a tutor's song
283          Using in vivo microdialysis in male zebra finches, we found that local estradiol levels incr
284                  In nightingales, but not in zebra finches, we found universal rhythm categories, wit
285 bilateral coordination for vocal learning in zebra finches, we investigated the anatomical organizati
286                                  In sleeping zebra finches, we observed slow wave sleep (SWS), rapid
287 ransported fluorescent tracers in adult male zebra finches, we show that Area X and other song contro
288                              Budgerigars and zebra finches were tested, using operant conditioning te
289                 In our first study, juvenile zebra finches were trained to perform one song and then
290                              Male and female zebra finches were treated with E2 or control vehicle fr
291   We identified a vocal-motor pathway in the zebra finch where memories that guide learning of song-e
292 regarious, non-territorial songbirds such as zebra finches, where females have access to numerous mal
293 in vivo imaging to measure spine dynamics in zebra finches, which learn to sing by imitating a tutor
294  manipulating the brain activity of juvenile zebra finches, which learn to sing by memorizing and voc
295                            We deafened adult zebra finches, which rely on auditory feedback to mainta
296 vity in the auditory forebrain of awake male zebra finches while presenting rare repetitions of a sin
297          We evaluated this question in adult zebra finches, whose premotor neurons in the nucleus rob
298 ly from auditory neurons in awake adult male zebra finches with multiple microelectrodes during repea
299 on between two bird species, the chicken and zebra finch, with regard to sex bias of autosomal versus
300 of histone 4 lysine 16 (H4K16) near MHM, the zebra finch Z chromosome appears to lack the MHM sequenc

 
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